Lower Limb Amputation Knee

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Review clinical trials related to Lower Limb Amputation Knee. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Prosthetic Performance Enhancement Trial

The purpose of this research is to determine the feasibility of an uneven terrain walking program for lower limb prosthesis users. The training is designed to induce step-to-step variability during walking within a safe environment, with the aim of improving walking skill and confidence.

Participants needed: 35
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Nevada, Las VegasUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

lower limb amputation at ankle (Symes) level and above [+4]

leg/foot ulcer or other conditions that cause pain during weight-bearing [+4]

Status: Recruiting

Clinical and Functional Assessment of Patients With Transfemoral Amputation Treated With Osteointegrated Implant

Limb amputation is a traumatic event that significantly reduces the ability to perform daily activities, impairs mobility, and lowers quality of life. In Italy, approximately 4 million people live with disabilities, with 1.2 million having motor disabilities. Among lower limb amputees (around 200,000), most are elderly, with amputations due to diabetic or vascular issues. Other groups include middle-aged adults (often victims of workplace accidents) and young individuals (victims of traffic accidents). Post-amputation rehabilitation mainly involves the use of prostheses, which, however, can cause skin problems due to the socket (the part that anchors the prosthesis to the residual limb). Among patients using a socket, 34-63% develop chronic skin issues and pain. Complications include excessive sweating, sores, abscesses, and irritation. Additionally, daily volume changes in the residual limb and long-term weight fluctuations further complicate the use of conventional prostheses. In the last two decades, research groups, assisted by experienced surgeons, have worked to develop implant solutions that bypass the socket and address these issues. One such solution is osteointegrated prostheses, which use the principle of osteointegration to anchor the prosthesis directly to the bone of the residual limb. A metal stem is surgically inserted into the medullary canal of the residual limb and fixed through bone growth, establishing a direct connection between the amputated limb and the external prosthesis. Osteointegrated prostheses are widely accepted worldwide as a valid alternative to socket prostheses, especially for young and active individuals with transfemoral, transtibial, transhumeral, or transradial amputations not caused by vascular issues. The key benefit of osteointegration is the restoration of load alignment along the anatomical and mechanical axis, improving control of the residual limb during walking, as well as overall functional capacity and quality of life. Other advantages include greater stability, enhanced sitting comfort, a wider range of hip movement, faster attachment and detachment of the prosthesis, and improved body perception. Additionally, the direct contact between the metal stem and the bone generates sensory feedback (osteoperception), allowing the patient to better control the amputated limb by perceiving ground contact through vibrations transmitted to the bone. Osteointegration offers the only viable alternative for prosthetic use in patients with a short residual limb, where conventional socket prostheses would not be suitable.

Participants needed: 15
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Istituto Ortopedico RizzoliUpdated: Feb 17, 2026Locations: 1
Eligibility criteria

Subjects of both sexes, aged between 18 and 65 years; [+5]

Peripheral vascular diseases; [+18]

Status: Recruiting

Clinical Application Observation on the Evaluation of Phantom Limb Pain With the Suralis System

This study tests whether a vibration-based feedback device (Suralis) can reduce phantom limb pain in people with lower-leg amputations over 3 weeks. Participants wear the device daily and report pain levels, walking ability, and quality of life - with no known risks, as it's a CE-certified medical device. If pain improves, the study team will help participants apply for insurance coverage to keep using the system long-term. The goal is to offer a simple, non-drug option that may help ease chronic pain and improve daily function for amputees. Participation is voluntary and can be stopped anytime without affecting medical care.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: MedianUpdated: Jan 7, 2026Locations: 1
Eligibility criteria

Unilateral major lower-limb amputation (transtibial or transfemoral) [+4]

Unstable wound or skin condition at the residual limb [+4]

Status: Recruiting

Promoting Physical Activity Following Dysvascular Amputation

Loss of a lower limb due to diabetes can have a devastating impact on physical and mental health and quality of life. Individuals are at risk of other diseases such as cardiovascular disease, loss of the other limb and death. Physical activity can reduce risk of chronic disease and improve health outcomes; however, physical activity levels in people with limb loss are low, often due to reduced balance and walking ability. Rehabilitation services are not readily available and the cost of delivering such programs remains high. Working with individuals with lower limb amputation, we created a virtual, peer-led physical activity behaviour change intervention called IMproving Physical Activity through Coaching and Technology following Lower Limb Loss (IMPACT-L3). We will conduct a pilot study to assess feasibility and optimize design of a future trial of effectiveness.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: West Park Healthcare CentreUpdated: Feb 24, 2025Locations: 1
Eligibility criteria

Dysvascular LLA (LLA due to diabetes or vascular disease) [+5]

actively receiving rehabilitation services related to physical activity/mobility [+2]

Status: Recruiting

Self-Management for Amputee Rehabilitation Using Technology.

Lower Limb Amputations (LLAs) are a substantial burden on the Canadian health services with nearly 50,000 cases reported between 2006 and 2011. To address the challenging nature of a LLA (e.g., decreased mobility, pain, depression), patients need to go through extensive rehabilitation programs. Effective self-management programs can help those with LLA to monitor their own condition and improve their quality of life. However, a lack of self-management programs, a limited healthcare budget, and a decrease in quality of services (e.g. shorter lengths of stay for inpatients and rapid movement to outpatient services) pose further challenges for patients with LLA. Self-management programs can be provided to clients through online mobile technologies (e.g., tablet) and offer accessible, low-cost, and potentially augmentative rehabilitation after discharge, in both urban and rural areas. To address these needs, an online educational and training platform for individuals with LLA called, Self-Management for Amputee Rehabilitation using Technology (SMART) was designed and developed. SMART focuses on LLA education, prosthetic limb management, and weekly support of peers. It is monitored by a trainer through a website. SMART will be evaluated in men and women with LLA aged 50 years and over, admitted to prosthetic rehabilitation throughout BC and ON. SMART has the potential to influence a client's post-LLA needs with direct (e.g., individual's health) and indirect (e.g., healthcare utilization) benefits. The purpose of this randomized controlled trial is to evaluate the effect of SMART in community dwelling older adults with unilateral, above or below, knee amputation.

Participants needed: 82
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: University of British ColumbiaUpdated: Jul 23, 2024Locations: 1
Eligibility criteria

Has a unilateral LLA (transtibial or transfemoral) due to diabetes or vascular d... [+5]

Substantial health conditions (e.g., congestive heart failure, diagnosed dementi... [+2]